Ontology Browser

Term:
Synpolydactyly 2 (DOID:9001994)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
polydactyly +     
synpolydactyly +     
Aarskog syndrome +   
Absence of Tibia with Polydactyly  
acheiropody  
acrofacial dysostosis Rodriguez type 
acrofacial dysostosis, Patagonia type 
Acrootoocular Syndrome 
acrorenal syndrome +  
Anonychia-Ectrodactyly 
Anonychia-Onychodystrophy with Hypoplasia or Absence of Distal Phalanges 
asphyxiating thoracic dystrophy +   
Banki Syndrome 
Biemond Syndrome II 
brachydactyly type E1  
brachydactyly type E2  
Brachyphalangy, Polydactyly, and Tibial Aplasia/Hypoplasia 
Camptodactyly 1 
Camptodactyly Joint Contractures and Facial Skeletal Dysplasia 
Camptodactyly Syndrome Guadalajara Type 1 
Camptodactyly Syndrome Guadalajara Type 2 
Camptodactyly Taurinuria 
Camptodactyly Vertebral Fusion 
Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia 
camptodactyly-arthropathy-coxa vara-pericarditis syndrome  
Camptodactyly-Ichthyosis Syndrome 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
Camptosynpolydactyly, Complex  
CAPOS Syndrome  
Carnevale Hernandez Castillo Syndrome 
Catel Manzke Syndrome  
Charcot-Marie-Tooth Disease, Foot Deformity of 
Chitayat Meunier Hodgkinson Syndrome 
CHITAYAT SYNDROME  
Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 
Cleft Palate, Deafness, and Oligodontia 
Coffin-Siris syndrome +   
cold-induced sweating syndrome +   
Cortical Blindness, Retardation, and Postaxial Polydactyly 
Cranioacrofacial Syndrome 
Craniosynostosis, Adelaide Type 
Crossed Polydactyly, Type I  
Crossed Polysyndactyly 
Culler-Jones syndrome  
Dandy Walker Malformation Postaxial Polydactyly 
Daneman Davy Mancer Syndrome 
Deafness, Congenital Onychodystrophy, Recessive Form 
Desbuquois dysplasia +   
Digitorenocerebral Syndrome  
Digitotalar Dysmorphism 
Distal Symphalangism +   
Dwarfism Stiff Joint Ocular Abnormalities 
Dystelephalangy 
Ectodermal Dysplasia Alopecia Preaxial Polydactyly 
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 
Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy  
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3  
Ectrodactyly-Cleft Palate Syndrome 
Eiken Skeletal Dysplasia  
Extensor Tendons of Fingers, Anomalous Insertion of 
Facial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly 
Fairbank Disease 
Femur Bifid with Monodactylous Ectrodactyly 
Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome 
Frias Syndrome 
Fried Goldberg Mundel Syndrome 
Frints De Smet Fabry Fryns Syndrome 
Frontootopalatodigital Osteodysplasia 
Fuhrmann syndrome  
Game Friedman Paradice Syndrome 
Garret Tripp Syndrome 
Gingival Fibromatosis with Hypertrichosis and Mental Retardation 
Goodman Camptodactyly 
Gordon Syndrome  
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Hairy Palms and Soles 
hand-foot-genital syndrome  
Heart-Hand Syndrome, Slovenian Type  
Hecht Scott Syndrome 
Hirschsprung Disease Polydactyly Heart Disease 
Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly 
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect 
holoprosencephaly 9  
Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip/Palate  
hydrolethalus syndrome +   
Hypoplasia of Tibia with Polydactyly  
Jackson-Weiss Syndrome  
Johnson Munson Syndrome 
Keutel Syndrome  
Khalifa Graham Syndrome 
Kozlowski-Krajewska Syndrome 
Laurence Prosser Rocker Syndrome 
Laurin-Sandrow Syndrome  
Leri Pleonosteosis 
Liver Fibrocystic Disease and Polydactyly 
Macrodactyly of the Foot 
Macrodactyly of the Hand 
Mammary-Digital-Nail Syndrome 
Maroteaux Fonfria Syndrome 
McKusick Kaufman Syndrome  
Meckel syndrome 13  
Meckel syndrome 4  
Meckel-Like Cerebrorenodigital Syndrome 
Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome +   
Metacarpal 4 5 Fusion  
Metaphyseal Acroscyphodysplasia 
Metatarsus Varus, Type I 
Mexican Cardiomelic Dysplasia 
Michels Caskey Syndrome 
Microcephaly with Mental Retardation and Digital Anomalies  
Microcephaly, Microphthalmia, Ectrodactyly of Lower Limbs, and Prognathism  
Mononen-Karnes-Senac syndrome 
Monophalangy of Great Toe 
Morillo-Cucci Passarge Syndrome 
Muller Barth Menger Syndrome 
Neurofaciodigitorenal Syndrome 
Nicolaides Baraitser Syndrome  
oculodentodigital dysplasia +   
Oculootoradial Syndrome  
Odontotrichoungual-Digital-Palmar Syndrome 
Oliver Syndrome 
Oroacral Syndrome, Verloes-Koulischer Type 
Oslam syndrome 
Oto-Palato-Digital Syndrome Type 1  
Oto-Palato-Digital Syndrome, Type 2  
Otopalatodigital Spectrum Disorder  
Pallister-Hall syndrome +   
Partial Aphalangia with Syndactyly and Duplication of Metatarsal IV 
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies 
Pfeiffer Mayer Syndrome 
Pfeiffer Tietze Welte Syndrome 
Polydactyly Myopia Syndrome 
Postaxial Polydactyly, Type A1  
Postaxial Polydactyly, Type A2 
Postaxial Polydactyly, Type A3 
Postaxial Polydactyly, Type A4 
Postaxial Polydactyly, Type A6  
Postaxial Polydactyly, Type A7  
Postaxial Polydactyly, Type A8  
Postaxial Polydactyly, Type A9  
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Preaxial Deficiency, Postaxial Polydactyly and Hypospadias  
Preaxial Hallucal Polydactyly 
Preaxial Polydactyly II  
Preaxial Polydactyly, 4  
Preaxial Polydactyly, III 
Preaxial Polydactyly, Type 1 
Progeroid Facial Appearance with Hand Anomalies 
Pseudotrisomy 13 Syndrome 
Radial Defect Robin Sequence 
Radio-Ulnar Synostosis Type 1 
Radio-Ulnar Synostosis Type 2 
Ray Peterson Scott Syndrome 
Rhizomelic Dysplasia Patterson Lowry Type 
Richieri Costa Guion-Almeida Syndrome 
Richieri Costa Pereira Syndrome  
Rozin Hertz Goodman Syndrome 
Saal Bulas Syndrome 
Sanderson Fraser Syndrome 
Sandhaus Ben-Ami Syndrome 
Santos Mateus Leal Syndrome 
Santos Syndrome 
Say Field Coldwell syndrome 
Scalp Defects Postaxial Polydactyly 
Schinzel-Giedion Syndrome  
Second Metatarsal-Metacarpal Syndrome 
Split Hand Split Foot Nystagmus 
split hand-foot malformation 1 with sensorineural hearing loss  
SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY  
Spondylocamptodactyly 
Stoll Alembik Dott Syndrome 
Symphalangism with Multiple Anomalies of Hands and Feet 
Symphalangism, C. S. Lewis Type 
Syndactyly, Type IV  
Syndactyly-Polydactyly-Earlobe Syndrome 
Synostosis, Carpal, with Dysplastic Elbow Joints and Brachydactyly  
Synpolydactyly 1  
Synpolydactyly 2  
Synpolydactyly 3 
Synpolydactyly with Foot Anomalies  
Tabatznik Syndrome 
Talipes +   
Talonavicular Coalition 
Tarsal Coalition 
tarsal-carpal coalition syndrome  
Teebi Kaurah Syndrome 
Teebi Syndrome 
Tel Hashomer Camptodactyly Syndrome 
Terminal Osseous Dysplasia and Pigmentary Defects  
Thai Symphalangism Syndrome 
Tibia Absent Polydactyly Arachnoid Cyst 
Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomalies 
Tollner Horst Manzke Syndrome 
trichorhinophalangeal syndrome type III  
Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet 
Triphalangeal Thumb +   
Tukel Syndrome 
Ulnar Hypoplasia Lobster Claw Deformity of Feet 
Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia 
Unilateral Adactylia 
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 
Urioste Martinez-Frias Syndrome 
Van Maldergem syndrome +   
Ventricular Extrasystoles Perodactyly Robin Sequence 
Vertical Talus, Congenital  
Vohwinkel Syndrome  
Walbaum Titran Durieux Crepin Syndrome 
Weaver syndrome  
Weyers Ulnar Ray/Oligodactyly Syndrome 
Zechi-Ceide Syndrome 
Zimmerman Laband Syndrome  

Synonyms
Exact Synonyms: SPD2 ;   SYNPOLYDACTYLY, 3/3-PRIME/4, ASSOCIATED WITH METACARPAL AND METATARSAL SYNOSTOSES
Primary IDs: MESH:C564278
Alternate IDs: OMIM:608180 ;   RDO:0013300

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.